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INSTRUCTION FOR USE: HOSPIQUICK 25 AIR, 25 O2
1. FOREWORD
GCE Medical Regulators are medical devices classified as class IIa
according to the Medical Device Directive 93/42/EEC.
Their Compliance with essential requirements of 93/42/EEC Medical
Device Directive is based upon EN 10524-4 standard.
EN
This instruction for use covers essential information for the whole life cycle
of the regulators:
•
Operation
•
Cleaning
2. INTENDED USE
MEDIFLOW
intended for the administration of the following medical gases in the
treatment, management, diagnostic evaluation and care of patients:
•
oxygen;
•
oxygen-enriched air;
•
nitrous oxide;
•
medical air;
•
synthetic air;
The product is not intended to be use with air or nitrogen for driving
surgical tool.
This low pressure regulator is intended to be fitted to medical gas pipeline
system terminal units in hospital or ambulance car or to quick connector
outlet of medical regulator, with nominal pressures up to 800 kPa.
3. OPERATIONAL, TRANSPORT AND STORAGE
SAFETY REQUIREMENTS
Keep away the product and its associated equipment from:
• heat sources (fire, cigarettes, etc.),
• flammable materials,
• oil or grease
• water
• dust
The product and its associated equipment must be prevented from
falling over.
Use only the product and its associated equipment in well vented area.
Always maintain oxygen cleanliness standards.
ULTRA is a low pressure regulator with flow-selector device
®
•
Maintenance
•
Disposal
•
carbon dioxide;
•
helium;
•
xenon;
•
specified
gases listed above.
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